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Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell
BACKGROUND: Soshiho-tang (SST) is a traditional medicine widely used for the treatment of chronic hepatitis. SST has been shown to confer a variety of pharmacological activities, including prevention of hepatotoxicity, promotion of liver regeneration, and modulation of liver fibrosis. In this study,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942327/ https://www.ncbi.nlm.nih.gov/pubmed/24580756 http://dx.doi.org/10.1186/1472-6882-14-78 |
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author | Lee, Jung-Jin Kwon, Hyeeun Lee, Ji-Hye Kim, Dong-Gun Jung, Sang-Hyuk Ma, Jin Yeul |
author_facet | Lee, Jung-Jin Kwon, Hyeeun Lee, Ji-Hye Kim, Dong-Gun Jung, Sang-Hyuk Ma, Jin Yeul |
author_sort | Lee, Jung-Jin |
collection | PubMed |
description | BACKGROUND: Soshiho-tang (SST) is a traditional medicine widely used for the treatment of chronic hepatitis. SST has been shown to confer a variety of pharmacological activities, including prevention of hepatotoxicity, promotion of liver regeneration, and modulation of liver fibrosis. In this study, we investigated the antiproliferative activity of native and fermented (FSST) formulations of SST in vascular smooth muscle cells (VSMCs) and examined the potential underlying mechanisms driving these effects. METHODS: SST, along with preparations fermented with Lactobacillus plantarum KFRI-144 (S-A144), L. amylophilus KFRI-161 (S-A161) and L. bulgaricus KFRI-344 (S-A344), were investigated to determine their effects on the proliferation and viability of VSMCs, along with the signalling pathways underlying these effects. RESULTS: S-A144 exhibited a strong, dose-dependent inhibition of VSMC proliferation relative to untreated controls, but the others did not affect. In addition, S-A144 significantly decreased the phosphorylation of Akt and PLCγ1 in a dose-dependent manner and induced cell cycle arrest at the G(0)/G(1) phase characterised by decreased expression of CDKs, cyclins and PCNA. CONCLUSIONS: The findings suggest that S-A144 exhibit enhanced inhibition of PDGF-BB-induced VSMC proliferation comparison to S-AOR through the suppression of cell cycle progression and expression of cell cycle-related proteins, along with the downregulation of Akt phosphorylation. |
format | Online Article Text |
id | pubmed-3942327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39423272014-03-05 Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell Lee, Jung-Jin Kwon, Hyeeun Lee, Ji-Hye Kim, Dong-Gun Jung, Sang-Hyuk Ma, Jin Yeul BMC Complement Altern Med Research Article BACKGROUND: Soshiho-tang (SST) is a traditional medicine widely used for the treatment of chronic hepatitis. SST has been shown to confer a variety of pharmacological activities, including prevention of hepatotoxicity, promotion of liver regeneration, and modulation of liver fibrosis. In this study, we investigated the antiproliferative activity of native and fermented (FSST) formulations of SST in vascular smooth muscle cells (VSMCs) and examined the potential underlying mechanisms driving these effects. METHODS: SST, along with preparations fermented with Lactobacillus plantarum KFRI-144 (S-A144), L. amylophilus KFRI-161 (S-A161) and L. bulgaricus KFRI-344 (S-A344), were investigated to determine their effects on the proliferation and viability of VSMCs, along with the signalling pathways underlying these effects. RESULTS: S-A144 exhibited a strong, dose-dependent inhibition of VSMC proliferation relative to untreated controls, but the others did not affect. In addition, S-A144 significantly decreased the phosphorylation of Akt and PLCγ1 in a dose-dependent manner and induced cell cycle arrest at the G(0)/G(1) phase characterised by decreased expression of CDKs, cyclins and PCNA. CONCLUSIONS: The findings suggest that S-A144 exhibit enhanced inhibition of PDGF-BB-induced VSMC proliferation comparison to S-AOR through the suppression of cell cycle progression and expression of cell cycle-related proteins, along with the downregulation of Akt phosphorylation. BioMed Central 2014-02-28 /pmc/articles/PMC3942327/ /pubmed/24580756 http://dx.doi.org/10.1186/1472-6882-14-78 Text en Copyright © 2014 Lee et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Article Lee, Jung-Jin Kwon, Hyeeun Lee, Ji-Hye Kim, Dong-Gun Jung, Sang-Hyuk Ma, Jin Yeul Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell |
title | Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell |
title_full | Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell |
title_fullStr | Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell |
title_full_unstemmed | Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell |
title_short | Fermented soshiho-tang with Lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell |
title_sort | fermented soshiho-tang with lactobacillus plantarum enhances the antiproliferative activity in vascular smooth muscle cell |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942327/ https://www.ncbi.nlm.nih.gov/pubmed/24580756 http://dx.doi.org/10.1186/1472-6882-14-78 |
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